Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele
0 9 0 0 1 1.2E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 1.3E-02
CUI: C0162316
Disease: Iron deficiency anemia
Iron deficiency anemia
0 21 0 0 1 1.0E-02
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism
0 5 0 0 2 2.5E-02
CUI: C0392514
Disease: Hereditary hemochromatosis
Hereditary hemochromatosis
0 56 0 0 1 7.5E-03
CUI: C0398791
Disease: Nijmegen Breakage Syndrome
Nijmegen Breakage Syndrome
0 144 0 0 1 4.5E-03
CUI: C0919890
Disease: Hyperfibrinogenemia
Hyperfibrinogenemia
0 1 0 0 1 1.3E-02
CUI: C1321551
Disease: Shprintzen-Goldberg syndrome
Shprintzen-Goldberg syndrome
0 21 0 0 2 2.1E-02
CUI: C1333763
Disease: Gastric Cardia Carcinoma
Gastric Cardia Carcinoma
0 13 0 0 1 1.1E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 1.3E-02
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 1.3E-02
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis
0 2 0 0 1 1.3E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 1 1.3E-02
CUI: C0000822
Disease: Abortion, Tubal
Abortion, Tubal
109 0 1 5.9E-03 0 0
CUI: C0000846
Disease: Agenesis
Agenesis
161 0 1 4.5E-03 0 0
CUI: C0001080
Disease: Achondroplasia
Achondroplasia
46 0 1 9.3E-03 0 0
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic
209 0 1 3.7E-03 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic
11 0 1 1.4E-02 0 0
CUI: C0001342
Disease: Acute periodontitis
Acute periodontitis
130 0 1 5.2E-03 0 0
CUI: C0001614
Disease: Adrenal Cortex Diseases
Adrenal Cortex Diseases
13 0 1 1.4E-02 0 0
CUI: C0001621
Disease: Adrenal Gland Diseases
Adrenal Gland Diseases
9 0 1 1.4E-02 0 0
CUI: C0001723
Disease: Affective Disorders, Psychotic
Affective Disorders, Psychotic
17 0 1 1.3E-02 0 0
CUI: C0001733
Disease: Afibrinogenemia
Afibrinogenemia
9 0 1 1.4E-02 0 0
CUI: C0001824
Disease: Agranulocytosis
Agranulocytosis
55 0 1 8.6E-03 0 0
CUI: C0001925
Disease: Albuminuria
Albuminuria
76 0 1 7.3E-03 0 0